One-Way valve Prosthesis for Percutaneous Placement Within the Venous System

• US 20100131049A1
• Filed: 11/24/2008
• Published: 05/27/2010
• Est. Priority Date: 11/24/2008
• Status: Abandoned Application

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Perkins, D.H., Thompson, Dustin
• Application Number:
  US12/276,866
• Publication Number:
  US 20100131049A1
• Time in Patent Office: Days
• US Class Current: 623/1.240
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2/2412 with soft flexible valve members, e.g. tissue valves shaped like natural valves check valves with flexible valve members in general F16K15/14
• CPC Class Codes: A61F 2/2436 Deployment by retracting a sheath
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2002/068 Modifying the blood flow model, e.g. by diffuser or deflector

Abstract

A one-way valve prosthesis for percutaneous placement within a vein, the valve including a valve body having an inlet and an outlet with a lumen that extends there between. The valve body is operable to alternate between a closed configuration wherein the valve body has a double cone shape and an open configuration wherein the valve body has a double frustoconical shape. A valve seat if formed within the lumen of the valve body at a midsection thereof. The valve seat is constricted to prevent flow there through when the valve body is in the closed configuration and the valve seat is open to allow flow there through when the valve body is in the open configuration. The valve seat opens in response to an actuation pressure and closes in the absence of the actuation pressure.

Claims

1. A one-way venous valve prosthesis for percutaneous placement within a vein comprising:

a valve body having an inlet and an outlet with a lumen that extends there between, the valve body being operable to alternate between

a closed configuration wherein the valve body has a double cone shape with apexes located at a midsection of the valve body, wherein a valve seat is defined within the lumen of the valve body at the midsection thereof, and

an open configuration wherein the valve body assumes a double frustoconical shape,

wherein the valve seat is constricted to prevent blood flow there through when the valve body is in the closed configuration and the valve seat is expanded to allow blood flow there through when the valve body is in the open configuration.

2. The venous valve prosthesis of claim 1, wherein the valve seat expands to the open configuration in response to an actuation pressure and wherein the valve seat closes to the closed configuration in the absence of the actuation pressure.

3. The venous valve prosthesis of claim 1, further comprising:

an annular self-expanding first anchor attached to the inlet; and

an annular, self-expanding second anchor attached to the outlet.

4. The venous valve prosthesis of claim 3, wherein the first and second anchors are nickel-titanium scaffolds.

5. The venous valve prosthesis of claim 1, wherein the valve body is formed from silicone.

6. The venous valve prosthesis of claim 1, wherein the valve body includes a first conical section and a second conical section, and the first conical section has a tapered wall thickness that continually decreases from the inlet to the midsection of the valve body and the second conical section has a tapered wall thickness that continually increases from the midsection of the valve body to the outlet.

7. The venous valve prosthesis of claim 6, wherein the second conical section includes a more gradual taper than the first conical section such that, when considered as a whole, the wall thickness of the outlet is relatively less than the wall thickness of the inlet.

8. The venous valve prosthesis of claim 1, wherein a portion of the valve body adjacent the inlet and a portion of the valve body adjacent the outlet have a first stiffness and an intermediate portion between the inlet and outlet has a second stiffness, wherein the first stiffness is greater than the second stiffness.

9. The venous valve prosthesis of claim 1, further comprising:

an expandable annular band attached to an outside surface of the valve body around the midsection.

10. The venous valve prosthesis of claim 9, wherein the expandable annular band is formed from nickel-titanium.

11. The venous valve prosthesis of claim 1, wherein an intermediate portion between the inlet and outlet includes folds of material of the valve body.

12. A one-way venous valve prosthesis for percutaneous placement within a vein comprising:

a valve body having a first conical section with an inlet and a second conical section with an outlet and a lumen that extends between the inlet and the outlet, the valve body operable to alternate between a closed configuration wherein the valve body has a double cone shape with apexes located at a midsection of the valve body, wherein a valve seat is defined within the lumen of the valve body at the midsection thereof, and an open configuration wherein the valve body has a double frustoconical shape,

wherein the valve seat is constricted to prevent flow there through when the valve body is in the closed configuration and the valve seat is expanded to allow flow there through when the valve body is in the open configuration, and

wherein the first conical section has a tapered wall thickness that continually decreases from the inlet to the midsection of the valve body and the second conical section has a tapered wall thickness that continually increases from the midsection of the valve body to the outlet such that the valve seat expands to the open configuration in response to an actuation pressure and the valve seat closes in the absence of the actuation pressure.

13. The venous valve prosthesis of claim 12, wherein the second conical section includes a more gradual taper than the first conical section such that, when considered as a whole, the wall thickness of the outlet is relatively less than the wall thickness of the inlet.

14. The venous valve prosthesis of claim 12, further comprising:

an annular self-expanding first anchor attached to the inlet; and

an annular, self-expanding second anchor attached to the outlet.

15. The venous valve prosthesis of claim 12, wherein the valve body is formed from silicone.

16. A percutaneous method of repairing an insufficient native valve within a vein, the method comprising the steps of:

percutaneously introducing a delivery system having a valve prosthesis loaded thereon into the patient, wherein the valve prosthesis has a valve body including an inlet and an outlet with a lumen that extends there between, the valve body operable to alternate between a closed configuration wherein the valve body has a double cone shape with a valve seat defined within the lumen of the valve body at a midsection thereof, and an open configuration wherein the valve body has a double frustoconical shape, wherein the valve seat is constricted to prevent flow there through when the valve body is in the closed configuration and the valve seat is open to allow flow there through when the valve body is in the open configuration;

tracking the valve prosthesis to the insufficient native valve; and

implanting the valve prosthesis such that the valve body spans across the insufficient native valve.

17. The method of claim 16, wherein the valve seat expands to the open configuration in response to an actuation pressure and wherein the valve seat closes to the closed configuration in the absence of the actuation pressure.

18. The method of claim 16, wherein the valve prosthesis includes an annular self-expanding first anchor is attached to the inlet and an annular, self-expanding second anchor is attached to the outlet.

19. The method of claim 18, wherein the delivery system includes a retractable sheath and the step of implanting the valve prosthesis further includes retracting the sheath of the delivery system to expand the valve prosthesis within the vein.

20. The method of claim 18, wherein the step of implanting the valve prosthesis includes positioning the valve body to bypass the sinus of the insufficient native valve in order to prevent blood stasis and further deterioration of the insufficient native valve.